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Phenotypic Abnormality (PA): Abnormal cerebellum morphology

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + + 5:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + + 4:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + + 3:   Abnormality of brain morphology [HP:0012443] <13>(43|63) (53|34|15)
+ + 2:   Abnormality of hindbrain morphology [HP:0011282] <2>(5|5) (7|2|1)
+ 1:   Abnormality of the metencephalon [HP:0011283] <3>(5|5) (7|2|1)
0:   Abnormal cerebellum morphology [HP:0001317] <15>(5|5) (7|2|1)
- 1:   Cerebellar atrophy [HP:0001272] <6>(0|3) (1|0|0)
- 1:   Cerebellar malformation [HP:0002438] <4>(4|2) (5|1|1)
- 1:   Abnormality of the dentate nucleus [HP:0100321] <2>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the cerebellum [HP:0007360] <2>(0|1) (1|1|0)
- 1:   Cerebellar dysplasia [HP:0007033] <2>(0|0) (0|0|0)
- 1:   Abnormal morphology of the cerebellar cortex [HP:0031422] <1>(0|0) (0|0|0)
- 1:   Cerebellar calcifications [HP:0007352] <1>(0|0) (0|0|0)
- 1:   Cerebellar edema [HP:0030915](0|0) (0|0|0)
- 1:   Cerebellar gliosis [HP:0012698](0|0) (0|0|0)
- 1:   Cerebellar hemangioblastoma [HP:0006880](0|0) (0|0|0)
- 1:   Dysplastic gangliocytoma of the cerebellum [HP:0500009](0|0) (0|0|0)
- 1:   Enlarged cerebellum [HP:0012081](0|0) (0|0|0)
- 1:   Fusion of the cerebellar hemispheres [HP:0006899](0|0) (0|0|0)
- 1:   Olivopontocerebellar atrophy [HP:0002542](0|0) (0|0|0)
- 1:   Rhombencephalosynapsis [HP:0031913](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARM repeat0.00002593Direct
WD40 repeat-like0.0002678Direct
Ypt/Rab-GAP domain of gyp1p0.02091Inherited
ARID-like0.04094Inherited
Nucleotide-diphospho-sugar transferases0.1321Inherited


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Clathrin adaptor core protein0.01165Inherited
Tetramerization domain of potassium channels0.0199Inherited
ARID domain0.02444Inherited
MIR domain0.04198Inherited
Class II aminoacyl-tRNA synthetase (aaRS)-like, catalytic domain0.05046Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
ARM repeat0.00001132Direct
WD40 repeat-like0.0001305Direct
Ypt/Rab-GAP domain of gyp1p0.01427Inherited
ARID-like0.02948Inherited
MIR domain0.04988Inherited
Class II aaRS and biotin synthetases0.05156Inherited
Nucleotide-diphospho-sugar transferases0.1066Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
47923,47923
  • 47923 - Ypt/Rab-GAP domain of gyp1p
  • 47923 - Ypt/Rab-GAP domain of gyp1p
  • 0.01427Inherited
    52374,47323
  • 52374 - Nucleotidylyl transferase
  • 47323 - Anticodon-binding domain of a subclass of class I aminoacyl-tRNA synthetases
  • 0.04988Inherited

    (show details)
    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.004427Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
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